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按需纳升级采样探针,用于采集脑积液。

On-Demand Nanoliter Sampling Probe for the Collection of Brain Fluid.

机构信息

Microsystems Laboratory 4 (STI-IEM-LMIS4), École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Laboratory of Molecular and Chemical Biology of Neurodegeneration (SV-BMI-LMNN), EPFL, 1015 Lausanne, Switzerland.

出版信息

Anal Chem. 2022 Jul 26;94(29):10415-10426. doi: 10.1021/acs.analchem.2c01577. Epub 2022 Jul 5.

Abstract

Continuous fluidic sampling systems allow collection of brain biomarkers . Here, we propose a new sequential and intermittent sampling paradigm using droplets, called Droplet on Demand (DoD). It is implemented in a microfabricated neural probe and alternates phases of analyte removal from the tissue and phases of equilibration of the concentration in the tissue. It allows sampling droplets loaded with molecules from the brain extracellular fluid punctually, without the long transient equilibration periods typical of continuous methods. It uses an accurately defined fluidic sequence with controlled timings, volumes, and flow rates, and correct operation is verified by the embedded electrodes and a flow sensor. As a proof of concept, we demonstrated the application of this novel approach and , to collect glucose in the brain of mice, with a temporal resolution of 1-2 min and without transient regime. Absolute quantification of the glucose level in the samples was performed by direct infusion nanoelectrospray ionization Fourier transform mass spectrometry (nanoESI-FTMS). By adjusting the diffusion time and the perfusion volume of DoD, the fraction of molecules recovered in the samples can be tuned to mirror the tissue concentration at accurate points in time. Moreover, this makes quantification of biomarkers in the brain possible within acute experiments of only 20-120 min. DoD provides a complementary tool to continuous microdialysis and push-pull sampling probes. Thus, the advances allowed by DoD will benefit quantitative molecular studies in the brain, i.e., for molecules involved in volume transmission or for protein aggregates that form in neurodegenerative diseases over long periods.

摘要

连续流体采样系统可用于采集脑生物标志物。在这里,我们提出了一种使用液滴的新的连续和间歇采样范例,称为按需液滴(DoD)。它在微制造神经探针中实现,并交替进行从组织中去除分析物和组织中浓度平衡的阶段。它允许定时、定量和流速受控的采样液滴加载来自脑细胞外液的分子,而没有连续方法典型的长瞬态平衡期。它使用具有精确定义的流体序列,并且通过嵌入式电极和流量传感器验证正确的操作。作为概念验证,我们展示了这种新颖方法的应用,以收集小鼠大脑中的葡萄糖,时间分辨率为 1-2 分钟,没有瞬态阶段。通过直接注入纳升电喷雾电离傅里叶变换质谱(nanoESI-FTMS)对样品中的葡萄糖水平进行绝对定量。通过调整扩散时间和 DoD 的灌注体积,可以调整在样品中回收的分子分数,以在准确的时间点反映组织浓度。此外,这使得在仅 20-120 分钟的急性实验中对脑内生物标志物进行定量成为可能。DoD 提供了一种与连续微透析和推挽采样探针互补的工具。因此,DoD 允许的进展将有益于大脑中的定量分子研究,即对于参与体积传递的分子或在神经退行性疾病中形成的蛋白质聚集体等在长时间内形成的分子。

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